Primary Device ID | 09348215045487 |
NIH Device Record Key | e6f603e2-20c5-4fed-a20c-da1064c99dd5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trial BiPolar Head |
Version Model Number | 112-24-0043 |
Company DUNS | 751993028 |
Company Name | SIGNATURE ORTHOPAEDICS PTY LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09348215045487 [Primary] |
HWT | Template |
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
Steralize Prior To Use | true |
Device Is Sterile | false |
[09348215045487]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-18 |
Device Publish Date | 2018-10-05 |
09348215045494 | 112-24-0044 |
09348215045487 | 112-24-0043 |
09348215045470 | 112-24-0042 |
09348215045654 | 112-24-0060 |
09348215045647 | 112-24-0059 |
09348215045630 | 112-24-0058 |
09348215045623 | 112-24-0057 |
09348215045616 | 112-24-0056 |
09348215045609 | 112-24-0055 |
09348215045593 | 112-24-0054 |
09348215045586 | 112-24-0053 |
09348215045579 | 112-24-0052 |
09348215045562 | 112-24-0051 |
09348215045555 | 112-24-0050 |
09348215045548 | 112-24-0049 |
09348215045531 | 112-24-0048 |
09348215045524 | 112-24-0047 |
09348215045517 | 112-24-0046 |
09348215045500 | 112-24-0045 |